Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021477808

FEI Number

3021477808

Entity Name

GREEN OR LLC

City/State/Country

Lakeville, MN, US

Establishment Address

17685 Juniper Path Ste 314, Lakeville, MN 55044, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

GREEN OR LLC (Owner Number: 10083909)

Owner / Operator Contact Address

17685 Juniper Path Ste 314, Lakeville, MN 55044, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Green OR Reprocessed Countersink Green OR Reprocessed ArthoCare Ablation Wand Green OR Reprocessed Reamer Green OR Reprocessed Burr, Orthopedic Green OR Reprocessed Blade, Saw, General & Plastic Surgery, Surgical Green OR Reprocessed DePuy Mitek Ablation Wand Green OR Reprocessed Instrument, Surgical, Orthopedic, AC-Powered Motor and Accessory/Attachement Green OR Reprocessed Orthopedic manual surgical instrument Green OR Reprocessed Bit, Drill Green OR Reprocessed Punch, Surgical Green OR Reprocessed Stylet, Surgical, General & Plastic Surgery Green OR Reprocessed Accessories, arthroscopic Green OR Reprocessed Blade, Scalpel Green OR Reprocessed ArthroCare ENT Coblator - private label Green OR Reprocessed Rasp Green OR Reprocessed Bur Green OR Reprocessed Retractor Green OR Reprocessed Staple, Removable (Skin) Green OR Reprocessed Passer

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HWW	Countersink	Orthopedic	Class 1	888.4540	2022-01-03
NUJ	Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed	General, Plastic Surgery	Class 2	878.4400	2022-01-03
HTO	Reamer	Orthopedic	Class 1	888.4540	2022-01-03
HTT	Burr, Orthopedic	Orthopedic	Class 1	888.4540	2022-01-03
GFA	Blade, Saw, General & Plastic Surgery, Surgical	General, Plastic Surgery	Class 1	878.4820	2022-01-03
NUJ	Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed	General, Plastic Surgery	Class 2	878.4400	2022-01-03
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2022-01-03
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2022-01-03
HWE	Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment	General, Plastic Surgery	Class 1	878.4820	2022-01-03
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2022-01-03
HTW	Bit, Drill	Orthopedic	Class 1	888.4540	2022-01-03
LRY	Punch, Surgical	General, Plastic Surgery	Class 1	878.4800	2022-01-03
GAH	Stylet, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2022-01-03
NBH	Accessories, Arthroscopic	Orthopedic	Class 1	888.1100	2022-01-03
GES	Blade, Scalpel	General, Plastic Surgery	Class 1	878.4800	2022-01-03
NUJ	Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed	General, Plastic Surgery	Class 2	878.4400	2022-01-03
HTR	Rasp	General, Plastic Surgery	Class 1	878.4800	2022-01-03
GFF	Bur, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4820	2022-01-03
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2022-01-03
GDT	Staple, Removable (Skin)	General, Plastic Surgery	Class 1	878.4760	2022-01-03
HWQ	Passer	Orthopedic	Class 1	888.4540	2022-01-03

Official Correspondent

Josh Kutzler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GREEN OR LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K953012	Boston Surgical Products, Inc.	DISPOSABLE & REUSABLE SURGICAL CUTTING TOOLS	1995-07-12
K970809	Somnus Medical Technologies, Inc.	BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL	1997-06-18
K222793	C.R. Bard, Inc.	WavelinQ Generator	2022-10-17
K002257	Tecno Instruments (Pvt.) , Ltd.	TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100	2000-10-19
K193591	Bowa-Electronics GmbH & Co. KG	ARC 400	2020-04-02

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0021-2015	Biomet, Inc.	1	Compress Face Reamer Product Usage: Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement, tumor resections, revision of previously failed total joint arthroplasty, and trauma.
Z-0031-06	Rita Medical Systems	2	Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826
Z-0041-05	Linvatec Corp.	2	Ultra Power Burs, Sterile, Single-Use.
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486

Similar Registrations

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3006272282	HG Medical GmbH	Raisting Bavaria, DE
8043496	REDA INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021477808. Last updated year: 2026. Please use registration number 3021477808 when referencing this establishment in official correspondence.